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Clinical Trials/NCT05928715
NCT05928715Enrolling By InvitationNot Applicable

Effect of Finger Feeding on Term Newborns: A Randomized Controlled Study

Amasya University1 site in 1 country140 target enrollmentStarted: April 15, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
140
Locations
1
Primary Endpoint
Expressed breast milk

Study Overview

Brief Summary

With the planned study, it was aimed to determine the effect of finger feeding method on newborns in term babies.

Detailed Description

It was planned as a randomized controlled experimental study design.

Full randomization will be performed and infants who meet the inclusion criteria will be assigned to groups by flipping a coin.

On the toss of a coin, if heads came up then subject was allocated to the control group. If tails came up, then subject was allocated to the intervention group. This procedure was repeated for each mother.

Within the scope of the study, "Informed consent" will be obtained from the parents for infants who need formula supplementation or for infants fed with expressed breast milk by the decision of the Physician in the experimental and control groups.

Babies in the control group will continue to receive routine care and no intervention will be made on their feeding style. The researcher will be informed verbally and practically about the finger feeding method and the application steps to the mothers of the babies in the experimental group and to the family members who will support their feeding in baby care. In this direction, it will be ensured that expressed breast milk or formula support is given by finger feeding method.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Mother is 18 years or older Newborns 38 weeks and older Newborns who do not have any postnatal health problems and are followed up with the mother Babies taking formula supplements Babies who have difficulty breastfeeding There is no obstacle to breastfeeding or breastfeeding

Exclusion Criteria

  • •Babies with sucking and swallowing dysfunction Babies with respiratory distress (respiratory rate over 60/min, babies with groaning, nasal wing breathing)

Arms & Interventions

Experimental group

Experimental

It is the group that will receive breast milk or formula by finger feeding.

Intervention: Finger feeding (Other)

Control group

No Intervention

No Intervention: control group attempt will not be implemented

Outcomes

Primary Outcomes

Expressed breast milk

Time Frame: 15 days after the start of the intervention

amount of daily expressed breast milk intake

finger feeding

Time Frame: 15 days after the start of the intervention

number of finger feeding per day

Formula intake

Time Frame: 15 days after the start of the intervention

amount of daily formula consumption

Breastfeeding

Time Frame: 15 days after the start of the intervention

Number of breastfeeding per day

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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